RGD:28902456 Rat Genome Database

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Variant: RGD:28902456 -  Homo sapiens

RGD ID: 28902456
RS ID: rs1840389903
ClinVar ID: CV868478
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MBL2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 54,531,200
GRCh38 10 52,771,440
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_154t1:c.187+9T>C
NM_000242.3:c.187+9T>C
NM_001378373.1:c.187+9T>C
NM_001378374.1:c.187+9T>C
More... 		01/12/2018 intron variant uncertain significance Chronic infections, due to MBL deficiency; LECTIN COMPLEMENT ACTIVATION PATHWAY, DEFECT IN, 1; Mannose-binding protein deficiency; MBL DEFICIENCY; MBL2 DEFICIENCY; MBP DEFICIENCY
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MBL2
Accession:NM_001378373
Location:INTRON

Gene Symbol:MBL2
Accession:NM_001378374
Location:INTRON

Gene Symbol:MBL2
Accession:NM_000242
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001104673 CLINVAR
dbSNP (RS) rs1840389903 CLINVAR
MedGen C3280586 CLINVAR
NCBI Gene MBL2 CLINVAR
OMIM 154545 CLINVAR
  614372 CLINVAR